| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105532041-105532238 | Common:2; Rare:49 | ||||
| chr7:105691170-105691283 | Rare:20 | ||||
| chr7:105691428-105691569 | Rare:20 | ||||
| chr7:105691722-105691888 | Common:4; Rare:33 | ||||
| chr7:106865545-106865692 | Common:1; Rare:30 | ||||
| chr7:107168858-107169035 | Rare:69 | ||||
| chr7:107563881-107564021 | Common:2; Rare:82; Clinvar (benign):3 | ||||
| chr7:107580126-107580285 | Common:2; Rare:62 | ||||
| chr7:107744039-107744208 | Rare:61 | ||||
| chr7:107891058-107891241 | Rare:87; Clinvar (benign):2 | ||||
| chr7:108526039-108526479 | Common:5; Rare:131 | ||||
| chr7:108569576-108569970 | Common:1; Rare:146 | ||||
| chr7:116862354-116862609 | Common:2; Rare:97 | ||||
| chr7:118183916-118184203 | Common:3; Rare:116 | ||||
| chr7:120951002-120951191 | Common:1; Rare:79 |